TW396087B - Laping tape - Google Patents

Laping tape Download PDF

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Publication number
TW396087B
TW396087B TW087104476A TW87104476A TW396087B TW 396087 B TW396087 B TW 396087B TW 087104476 A TW087104476 A TW 087104476A TW 87104476 A TW87104476 A TW 87104476A TW 396087 B TW396087 B TW 396087B
Authority
TW
Taiwan
Prior art keywords
honing
layer
molecular weight
belt
resin
Prior art date
Application number
TW087104476A
Other languages
Chinese (zh)
Inventor
Kasao Okada
Shigeo Kurose
Original Assignee
Tdk Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Tdk Corp filed Critical Tdk Corp
Application granted granted Critical
Publication of TW396087B publication Critical patent/TW396087B/en

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D11/00Constructional features of flexible abrasive materials; Special features in the manufacture of such materials
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/127Structure or manufacture of heads, e.g. inductive
    • G11B5/187Structure or manufacture of the surface of the head in physical contact with, or immediately adjacent to the recording medium; Pole pieces; Gap features
    • G11B5/1871Shaping or contouring of the transducing or guiding surface
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24BMACHINES, DEVICES, OR PROCESSES FOR GRINDING OR POLISHING; DRESSING OR CONDITIONING OF ABRADING SURFACES; FEEDING OF GRINDING, POLISHING, OR LAPPING AGENTS
    • B24B21/00Machines or devices using grinding or polishing belts; Accessories therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D11/00Constructional features of flexible abrasive materials; Special features in the manufacture of such materials
    • B24D11/001Manufacture of flexible abrasive materials
    • B24D11/005Making abrasive webs
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/34Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents characterised by additives enhancing special physical properties, e.g. wear resistance, electric conductivity, self-cleaning properties
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/84Processes or apparatus specially adapted for manufacturing record carriers
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/41Cleaning of heads
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24355Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
    • Y10T428/24372Particulate matter
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24355Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
    • Y10T428/24372Particulate matter
    • Y10T428/2438Coated
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24355Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
    • Y10T428/24372Particulate matter
    • Y10T428/24405Polymer or resin [e.g., natural or synthetic rubber, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24355Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
    • Y10T428/24372Particulate matter
    • Y10T428/24421Silicon containing

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Polishing Bodies And Polishing Tools (AREA)
  • Laminated Bodies (AREA)
  • Paints Or Removers (AREA)

Abstract

This is a lapping tape with a lapping layer on a flexible substrate. It has inorganic powders and a binder as main components. The binder contained in the lapping layer has (1) a phenoxy resin, and (2) a polyester polyurethane resin with a number-average molecular weight Mn not less than 20000 but not greater than 100000. Accordingly, the obtained lapping tape exhibits excellent prevention of lapping scratches generation on the surface to be lapped. The lapping layer peeling from the lapping tape can be suppressed; the lapping tape has excellent lapping ability.

Description

A 7 B7 五、發明説明(I ) 本發明係有關用於磁頭、磁碟片等之表面硏磨之硏磨 帶者》 先行技術中,磁頭之精密加工、磁氣記錄媒體表面之 加工上於彎曲性支撑體上使用具硏磨層之硏磨帶。硏磨層 係將硏磨層形成用塗料塗於彎曲性支撑體上之後,經乾燥 後形成之,硏磨層形成用塗料中以含氧化鋁、氧化鉻、碳 化矽、氧化鐵、氮化矽、金鋼石f之無機質粉體;氯化乙 烯系樹脂、聚酯系樹脂、聚胺酯系樹脂等之有機質粘合劑 (粘著劑);以及其他配合劑等混煉,分散之狀態者。 先行技術中公知i硏磨帶之製造方法者有特開平5 -1 9 2 8 6 9號公報所載之方法,該方法係利用含特定結 構式組成重覆單位之平均分子量1 0 0 0〜1 0 0 0 0之 環氧樹脂與含多官能異氰酸酯之塗料,以及數平均分子量 5 ◦ 0 〇〜2 0 0 0 0之末端具0H基之聚胺酯樹脂使用 後製造硏磨帶之方法。該製造方法藉由組合上述各樹脂使 用後,儘管交聯反應溫度降至室溫亦可充份取得交聯反應 速度,且具高度交聯密度。 經濟部中央標準局員工消費合作社印製 -----.---C ...裝 ΙΓ -'· (請先閲讀背面之注意事項再填:¾本頁) 又,特開平5 - 1 9 2 8 7 0號公報公開有由含特定 結構式組成重覆單位之平均分子量1 0 0 0〜5 0 0 0 0 之環氧樹脂與於數平均分子量1 0 0 0 0〜3 0 0 0 0之 末端具OH基之玻璃轉移點(Tg)爲_20°C〜40°C 之聚酯樹脂與使用.含多官能異氰酸酯之塗料之硏磨帶之製 造方法。而藉由使用此樹脂後,可於反應硬化中減少產生 不齊之品質被報告指出》 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)·4 - 經濟部中央標準局員工消費合作社印製 A7 _ B7 五、發明説明g ) 惟,該任一提案中,做爲硏磨帶並無充分之塗膜強度 可言,於硏磨試驗中癘有出現硏磨層塗膜之掉落極不理想 〇 本發明則針對此不理想點以硏磨磁頭、磁碟片等表面 •—-- ... 時,具均衡良好之充份可做爲硏磨帶功能之硏磨帶之硏發 爲目的,亦即提供可完全防止產生於硏磨對象表面之硏磨 刮傷者,具充份之塗膜強度之減少刮傷硏磨帶之硏磨層同 時可提供優異之硏_磨功能之硏磨帶者。 爲解決本發明課題,本發明者針對可用於硏磨帶之結 合組成做精密硏討之結果,發現藉由苯氧基樹脂與特定分 子量之聚酯聚胺醋樹脂之含有混合物之結合劑使用後,可 有效解決該問題點,進而完成了本發明。 亦即,本發明於彎曲性支.撑體上以含無機質粉體及結 合劑做爲主成份之具硏磨層之硏磨帶中,所含該硏磨層之 結合劑者係由含1 )苯^氧基樹脂與,2 )'數平均分子量Μ η爲2 0 〇 〇 〇 $ Μ n S 1 〇 〇 〇 〇之聚酯聚胺酯樹脂所 組成者。 另外,本發明較佳形態係由苯氧基樹脂之數平均分子 量1 0 0 0 0以上^所組成者。 又,本發明較佳形態係由苯氧基樹脂之數平均分子量 爲1 0 0 0 0以上3 0 0 0 0以下所組成者。 又,本發明理.想形態係由苯氧基樹脂與聚酯聚胺酯樹 脂之重量配合比例爲5 : 9 5〜7 0 3 Q者所形成者。A 7 B7 V. Description of the invention (I) The present invention relates to honing belts for surface honing of magnetic heads, magnetic disks, etc. In the prior art, the precision processing of magnetic heads and the processing of the surface of magnetic recording media are on A honing belt with a honing layer is used on the flexible support. The honing layer is formed by applying a coating for forming a honing layer on a flexible support and drying it. The coating for forming a honing layer contains alumina, chromium oxide, silicon carbide, iron oxide, and silicon nitride. 2. Inorganic powder of gangue f; organic binders (adhesives) such as vinyl chloride resins, polyester resins, polyurethane resins, etc .; and other compounding agents such as kneaded and dispersed state. A known method for manufacturing i honing belts in the prior art is a method described in Japanese Patent Application Laid-Open No. 5 -1 9 2 8 6 9 which uses an average molecular weight of a repeating unit composed of a specific structural formula 1 0 0 0 ~ A method for manufacturing a honing belt after using an epoxy resin of 1 0 0 0 0, a coating containing a polyfunctional isocyanate, and a polyurethane resin having a number average molecular weight of 5 0 0 to 2 0 0 0 at the end. In this manufacturing method, after using the above-mentioned resins in combination, the crosslinking reaction speed can be sufficiently obtained even if the crosslinking reaction temperature is lowered to room temperature, and has a high crosslinking density. Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs -----.--- C ... equipment ΙΓ-'· (Please read the notes on the back before filling: ¾ this page) Also, JP 5-1 No. 9 2 8 7 0 discloses an average molecular weight of 1 0 0 0 to 5 0 0 0 0 and an average molecular weight of 1 0 0 0 to 3 0 0 0. Polyester resin with a glass transition point (Tg) at the end of 0 of OH group of _20 ° C ~ 40 ° C and a method for manufacturing a honing belt for a coating containing a polyfunctional isocyanate. After using this resin, it can reduce the uneven quality in the reaction hardening. It is reported that the paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm). 4-Consumption by employees of the Central Standards Bureau of the Ministry of Economic Affairs Cooperative printed A7 _ B7 V. Description of the invention g) However, in any of these proposals, there is no sufficient coating film strength as a honing belt. In the honing test, the coating film of the honing layer did not appear. The falling pole is not ideal. The present invention aims at this unsatisfactory point when honing magnetic heads, magnetic discs and other surfaces... ---, a well-balanced enough honing belt can be used as a honing belt. The purpose of hairpin is to provide those who can completely prevent the honing and scratching on the surface of the honing object, and have sufficient coating film strength to reduce the honing layer of the honing belt while providing excellent honing functions. The honing belt. In order to solve the problem of the present invention, the present inventor made a precise discussion on the bonding composition that can be used in the honing belt, and found that after using the binder containing a mixture of a phenoxy resin and a polyester polyurethane resin of a specific molecular weight , Can effectively solve this problem, and then complete the present invention. That is, in the present invention, a honing belt with a honing layer containing inorganic powder and a binder as a main component is used on a flexible support. The binder containing the honing layer is composed of 1 ) A phenoxy resin and 2) a polyester polyurethane resin having a number-average molecular weight M n of 20,000 $ M n S 10,000. In addition, a preferred aspect of the present invention is one in which the number average molecular weight of the phenoxy resin is 100 000 or more ^. In a preferred embodiment of the present invention, the number-average molecular weight of the phenoxy resin is 100 to 300. In addition, the present invention is intended to be formed by a weight ratio of a phenoxy resin to a polyester polyurethane resin of 5: 9 5 to 7 0 3 Q.

V 另外,本發明理想形態係由聚酯聚胺酯之玻璃轉移溫 ϋ張尺度適用中國國家標準(CNS ) Α4規格(210X297公釐)_ c - (請先閜讀背面之注意事項再填{:?本頁)V In addition, the ideal form of the present invention is that the glass transition temperature scale of polyester polyurethane is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) _ c-(Please read the precautions on the back before filling in {:? (This page)

經濟部中央標準局員工消費合作社印製 A 7 · B7 · 五、發明説明0 ) 度T g爲一 5 0 °C〜8 0 °C者所組成者。 又,本發明理想形態係由無機質粉體爲莫氏硬度5以 上,粒度爲0.1〜20#m者所組成者。 又,本發明理想形態係本發明硏磨帶以使用於磁頭、 磁碟片之硏磨者之組成者。 圖面之簡單說明 圖1係代表本發明硏磨帶之截面模式圖者。... . 以下,參照圖1做本發明理想實施形態詳細說明乏。 圖1中代表本發明硏磨帶之實施形態之模式截面圖。 本發明硏磨帶1係於彎曲性支撑體2上,爲硏磨磁頭 '、磁-碟-片等-表面(以下·稱「__被'硏胃-_」_)_所具備之硏磨.層 3。此硏磨層3中含硏磨材料之無機質粉體,與爲粘合此 無機質粉體之粘合劑。i ' . 本發明之硏磨層3係混合該無機質粉體與粘合劑以及 必要時使用之各種添加劑等(有機)溶劑混合分散之硏磨 \ · - 層形成用塗料塗於彎曲性支撑體2之上之後,乾燥而形成 者。 本發明所使用之、結合劑中以苯氧基樹脂,數平均分子Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs A 7 · B7 · V. Description of the invention 0) Degree T g is composed of 50 ° C ~ 80 ° C. In addition, an ideal form of the present invention is one in which the inorganic powder has a Mohs hardness of 5 or more and a particle size of 0.1 to 20 # m. In addition, an ideal form of the present invention is a composition of the honing belt of the present invention used for a honing head of a magnetic head or a magnetic disk. Brief Description of Drawings Fig. 1 is a schematic sectional view of a honing belt according to the present invention. .... Hereinafter, an ideal embodiment of the present invention will be described in detail with reference to FIG. 1. FIG. 1 is a schematic sectional view showing an embodiment of the honing belt of the present invention. The honing belt 1 of the present invention is attached to a flexible support 2 and is a surface provided by a honing magnetic head ', magnetic-disc-disc, etc. (hereinafter referred to as "__ 被' 硏 stomach -_" _) _磨. Layer 3. The honing layer 3 contains an inorganic powder of a honing material and a binder for bonding the inorganic powder. i '. The honing layer 3 of the present invention is a honing mixture in which the inorganic powder is mixed with a binder (and various organic solvents) and other (organic) solvents if necessary, and the coating is formed on a flexible support. After 2 times, it is dried and formed. In the present invention, a phenoxy resin is used in the binder, and the number average molecule is

- · S 量Μη爲200 0 OSMnSi 000 0 0之聚酯聚胺酯 樹脂做爲必須成份含有之。 本發明所使用.之苯氧基樹脂係由雙酚A與環氧氯丙烷 所合成之窩分子量聚羥基聚醚者,化學結構係與環氧樹脂 相同者,惟相較一般所使用之環氧樹聘,其分子量極大。 .'一 I In —m —Mt n I4H nn·— nt ^^'先閲請背兩之注意^項再填寫本頁). 本紙張尺度適用中國國家標準(CNS ) A4規格(2〗〇x29Tifrt ) ,g_ A7 B7 五、發明説明f ) 而本發明所使用之苯氧基樹脂之數平均分子量Μ η爲超過 10000者,特別以10000以上至30000以下 者爲理想適用者。若使用—般之環氧樹脂時’其數平均分 子量爲1 0 0 0 0以下,無法充份取得塗膜強度’易產生 硏磨層塗膜脫落等問題。其中平均分子量係藉由所謂之標 準聚苯乙烯法之測定方法所測之値者。 苯氧基樹脂係爲粘合劑總量辛5〜7 0重量% ’較佳 爲1 0〜6 0重量%,更理想者爲1 0〜5 0重量%含有 者。含量不足·5重量%時,硏磨層之塗膜強度將下降,硏 磨層塗膜之脫落等問題點將出現。反之,含量大於7 0重 量%時,則硏磨層之塗膜變硬變脆呈無柔軟性性狀態,造 成被硏磨物受損之起因。 本發明所使用之苯氧基其具體例如Phenoxy 八5 5〇0; — 6 5公司之苯氧基樹脂之「?尺11(:」、「 PKHH」、 「PKHJ」等例。此等均滿足上述理想數 平均分子量之範圍者。 i 經濟部中央標準局員工消費合作杜印製 (請先閱請背面之注意事項再填寫本頁) 本發明之硏磨層中做爲粘Λ合劑均~^^量 Μη 爲 20000SMnl00000,較佳者、爲 2 0 0 0 OSMnS 8 0 0 0 0之聚酯聚胺酯樹脂做爲必 須成份者。具亭該數平均分子量Μη之聚酯聚胺酯樹脂含 於硏磨層中者可提昇硏磨層形成用塗料之分散性使塗設形 成之硏磨層具優異之硏磨特性。 ' ( X , 聚酯聚胺酯樹脂之數平均分子量Μη不足2 0 0 0 0 Μ 大小使得硏磨層塗膜強度降低,硏磨層塗膜之膜落等問題 本紙張尺度適用中國國家標準(CNS ) Α4規格(210X297公釐)-7- 經濟部中央標準局員工消費合作社印製 A7 B7 五、發明説明戶) 產生。反之數平均分子量Μη大於1 〇 〇 〇 〇 〇之大値則 降低硏磨層形成用塗料之分散性導致硏磨層表面劣化,硏 磨操作時造成被硏磨物之損傷。 該聚酯聚胺酯樹脂之含量爲粘合劑中之3 0〜9 5重 量%、較佳爲4 0〜9 0重量%,更佳爲5 0〜9 0重量 %者。聚酯聚胺酯樹脂含量超出9 5重量%則硏磨層塗膜 強度下降,硏磨層塗膜脫落等缺嘻出現。反之含量小於3 0重量%則硏磨層之塗膜變硬變脆呈無柔軟性狀態,硏磨 操作時易造成被硏磨物之損傷。 又,聚酯聚胺酯樹脂之玻璃轉移溫度T g爲—5 0。(: STgS80°C,較佳者爲一5p°CSTgS + 4〇t:, 更理想者爲—4 5〇CSTgS+2 0t之範圍者。、當备璃 轉移溫度太低則硏磨層塗膜強度降低,硏磨能力下降。反 之玻璃轉移溫度T g太高則硏磨層塗膜變硬且脆,呈無柔 軟性狀態,硏磨操作時造成被硏磨物之損傷。 又,該樹脂之玻璃轉移1度T g係以動態粘彈性測定 裝置所測定之値。 本發明所使用之聚酯聚胺酯樹脂係將聚酯二醇於異冑 酸酯以及所期待之鏈延長劑等化合物共同反應者。 本發明所使用之聚酯聚胺酯樹脂係指將有機二異氰^ 酯(A )、分子量500〜50 0 0之聚酯二醇(B)、 分子量5 0 0以下之鏈延長劑((:)相互反應者。 聚酯聚胺酯樹脂之製造中所使用之有^二異氰酸醋( » A)之例如:2,4一甲苯醯二異氰酸酯、2,6 —甲苯 本紙張尺度適用中國國家標準(CNS > A4規格(210X 297公釐)_ ft - ' :- _____________丁 *. t {請先閲請背面之注t項再填&?本頁) · 經濟部中央標準局貝工消費合作社印製 A7 B7 五、發明説明-) 酿一異氰酸酯、對一苯烯二異氰酸酯、二苯基甲院二異氰 酸醋、間一苯烯二異氰酸酯、己亞甲基二異氰酸酯、四亞 甲基一異氯酸醋、3 ’ 3 —二甲氧基一4,4-—雙酣 二異氰酸酯、2,4-萘二異氰酸酯、3,3 --二甲基 一4 ’ 4 / 一雙苯烯二異氰酸酯、-4,4 < 一二苯烯二異 氰酸酯、4,4 / —二異氰酸酯二苯醚、1,5 —萘二異 氰酸酯、對—二甲苯二異氰酸酯、間一二甲苯二異氰酸醋 ' 1 ’ 3 —二異氰酸酯甲基環己院、1,4 —二異氰酸酯 甲基環己烷、4,4 / 一二異氰酸酯環己烷、4,4 -— 二異氰酸酯環己甲烷、異氟爾酮二異氰酸酯等例。 聚酯聚胺酯樹脂之製造中所使用之聚酯二醇(B )之 例係以分子量爲5 0 0〜5 0 0 0之範圍者。聚酯二醇之 羧酸成份之例如:對苯二甲酸、異苯二甲酸、鄰苯二甲酸 ' 1 ’ 5 —萘二甲酸等之芳香族二羧酸、對一氧基苯甲酸 、對-(羥基乙氧基)苯甲酸等之芳香族氧基羧酸;琥珀 酸、己二酸、壬二酸、癸二酸、月桂二羧酸等之脂肪族二 羧酸等例。其中又以對苯二甲酸、異苯二甲酸、鄰苯二甲 酸、’己二酸、癸二酸爲特別理想者。 又,聚酯二醇之甘醇成份例如:乙二醇、丙二醇、1 ,3—丙二醇、1,4 一丁二醇、1,_5 —戊二醇、1, 6 —己二醇、新戊二醇、二乙二醇、二丙二醇、2,2, 4 -三甲基一1,..3 —戊二醇、環己二甲醇、雙酚A之環 氧乙烷附加物及環氧丙烷附加物,氫化雙酚A之環氧乙烷 附加物及環氧丙烷附加物等等。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐)-9 - (諳先閱讀背面之注意事項再填寫本頁) 裝· 訂 A7 B7 經濟部中央標準局員工消費合作社印製 五 、發明説明P .) 1 1 該 聚酯 二 醇 其他例如 : δ — 己 內 酯 等 之 內 酯 類 經 開 TSt 壞 1 1 | 聚 合 後 取 得 之 內 酯 系 聚 酯 二 醇 類 等 例 〇 1 1 長 鏈 二 醇 ( B ) 如 上 所述 爲 提 高 聚 酯 聚 胺 酯 樹 脂 之 機 it 1 1 械特 性 之 聚 酯 二 醇 其分子 量 以 5. 0 0 5 0 0 0 者 使 用 先 閱 1 1 者 宜 〇 分 子 量 小於 5 0 0 則 胺 酯 基 之 濃 度 太 大 樹 脂 柔 軟 in 背 ι6 1 I 性 > 溶 劑 溶 解 性 降 低 產 生 不 良 情 況 0 反 之 分 子 量 太 大 超 之 注 意· 1 華 1 出 5 0 0 0 則 胺 酯 基 濃 度 太低 低 聚 酯 聚 胺 酯 樹 脂 之 特 項 再 1 有 強 韌 性 及 耐 磨 損 性 均 不 理 想 0 填 本 ; 裝 聚 酯 聚 胺 酯 樹 脂 之 製 造 時所使 用 之 該 分 子 量 小於 頁 1 1 5 0 0 之 鏈 延 長 劑 ( C ) 係 含 於 1 分子 中 2 個 以 上 活性 氫 1 1 、 S田 m 整 聚 酯 聚 胺 酯 樹 脂 中 之 胺 酯 基 或 尿 基 濃 度 後 於 聚 酯 1 聚 胺 酯 中 附與特有 強 韌 性效 ★ 果 者 〇 訂 I 鏈 延 長 劑 ( C ) 之 具 體 化 合物例如 乙 二 醇 、 1 3 1 1 I — 丙 二 醇 、 1 4 — 丁 二 醇 1 6 — 己 二 醇 > 環 己 二 甲 1 1 醇 二 甲 苯 二 醇 、 二 乙 二 醇 三 乙 二 醇 、 雙 酚 A 之 環 氧 乙 1 烷附加物 等 之 直 鏈 二 醇 > 丙 二 醇 新 戊 二 醇 > 1 2 一 丁 -* | — 醇 1 3 — 丁 二 醇 % 2 2 4 — 三 甲 基 一 1 3 _ 1 I 戊 二 醇 、 雙 酚 A 之丙 稀 氧 化物 附加物 之分枝 二 醇 單 乙 醇 1 1 I 胺 \ 正 一 甲 基 乙 醇 胺 等 之 胺 醇 、 乙 烯 二 胺 % 己 亞 甲 基 二 胺 1 > 異 氟 爾 酮 二 胺 等 之 二 胺或 氫 等 例 〇 1 1 而 理 想 用 於本 發 明 之 聚 酯 聚 胺 酯 樹 脂 之 例如 聚 酯 二 1 | 醇 ( 1 ) / 聚 酯 二 醇 ( 2 ) / 新 戊 二 醇 / 4 4 一 二 苯 1 I 基 甲 院 二 異 氰 酸 酯 之 反 應 生 成物 者 , 聚 酯 二 醇 ( 1 ) 之 例 1 1 I 如 : 對 苯 二 甲 酸 / 異 苯 二 甲 酸 / 乙 二 醇 / 新 戊 二 醇 1 1 本紙張尺度適用中國國家標準(CNS ) A4说格(210X297公釐)-10- 經濟部中央標準局員工消費合作杜印聚 A 7 B7 五、發明説明存) 50/50/50/50 莫耳比者,聚酯二酯(2 )之例如:己二酸 /1,4 — 丁二醇/新戊二醇=1〇 0/7 5/2 5 莫耳 比者。 又,藉由控制此聚酯二醇(1 )/聚酯二醇(2 )之 配合比率及胺酯基之濃度後,可任意控制聚酯聚胺酯樹脂 之玻璃轉移溫度Tg。 含於硏磨層(硏磨層形成用塗料)之該粘合劑量爲含 於硏磨層中1 0 0重量份無機質粉體之5〜5 0重量份, 特別以1 0〜'4 0重量份者佳。當粘合劑含量小於5重量 份時,將降低硏磨層之塗膜強度,而造成硏磨層之塗膜脫 落。反之,粘合劑含量大於5 0重量份則將降低無機質粉 體含量造成硏磨特性不良。 做爲硬化該結合劑之交聯劑之例以各種聚異氰酸酯, 特別以二異氰酸酯使用時,特別以1種以上之甲苯烯二異 氰酸酯、六亞甲基二異氰酸酯,亞甲基二異氰酸酯者爲宜 。該交聯劑以具有複數之三羥甲基丙烷等氫氧基者變性之 交聯劑或二異氰酸酯化合物3分子結合之三聚異氰酸酯型 交聯劑使用者爲特別理想者。該交聯劑係與含於該粘合劑 之官能基等相結合後之樹脂交聯者。交聯.劑之含量爲 1 0 0重量份結合劑之10〜3 0重量份者爲宜。硬化熱 硬化性樹脂中,逋常以於加熱烤箱4 0〜8 0 °C下加熱1 2〜4 8小時者即.可。 做爲含於硏磨層形成用塗料(硏磨層)中之必須成份 之無機質粉體以莫氏硬度5以上者使用者宜’例如:碳化 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)-11 - ~ 『,二 Γ m ml 1V1 I tm· —1 ^—fv I t 、T - (請先閱讀背面之注意事項再填1ΪΤ本頁) A7 ______ B7 五、發明説明$ ) 矽、氧化鋁、氮化矽、氧化鉻、氧化鉻、金鋼石、剛砂等 之微粉末以單獨或2種以上混合使用者。其中又以碳化矽 或氧化鋁使用者爲較理想者。 無機質粉體之粒徑爲0 . 1〜2 0 Am者宜,實用上 供應之具體粒徑者以選取含於實際之粗刮或加工硏磨用目 的者即可。未滿0. 1 Am之粒徑則加工硏磨用其硏磨功 能將不足,反之大於2 0 /zm易準成粗刮用時被硏磨物受 損之問題點出現。 又’本發,之硏磨層中,做爲必要時添加劑之具潤滑 效果、靜電防止效果、分散效果、可塑效果等所使用者, 其具體例以脂肪酸、脂肪酸酯、聚矽氧油類、氟油、各種 界面活性劑,炭黑等可添加之。 經濟部中央標準局員工消費合作社印製 ---^------' . 一裝-- -'- (锖先閱讀背面之注意事項再填??本頁) 做爲硏磨層形成用塗料所使用之有機溶劑者如:丁酮 、甲基異丁酮、環己酮等酮類、甲苯、二甲苯等之芳香族 烴基類、醋酸乙酯、醋酸丁酯等酯類以單一溶劑或此等任 意比率之混合溶劑使用之。其中又以含環己酮之高沸點溶 劑者因可形成良質之硏磨層者爲較佳。環己酮以含於全有 機溶劑之2 0〜6 0重量%,較佳者爲2 5〜5 0重量% 者佳。於此範圍中可取得良好之硏磨層表面性,提昇硏磨 功能,更可預防硏磨層刮傷之產生。 該硏磨層形成用塗料之固形份濃度以3 0〜7 0重量 %者宜,較佳者爲.4 0〜6 0重量%者,此値若小於3 0 重量%時,則硏磨層中之殘留溶劑量將增加,無法取得均 勻之塗膜等不理想狀態。反之,大於7 0重量%時,則塗 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)-12 · 經濟部中央標準局員工消費合作社印裝 A7 B7 五、發明説明彡〇 ) 料粘度提昇,硏磨層之塗膜乾燥速度太快而無法取得均句· 塗膜呈不理想狀態。 硏磨層3之膜厚度依其被硏磨物之形狀、材質等而選. 取,一般以3〜25/zm,更理想者爲5〜20em者。 不足3 之膜厚度因膜厚度太薄將使塗膜之彈力性消失 。硏磨操作過程易損及被硏磨物。反之,太大超出2 5 # m時,硏磨操作時易產生硏磨-之刮傷。硏磨層3 —般 以單獨塗佈形成者,亦可2層以上之複數層者。 本發明所使用彎曲性支撑體2可使用聚乙烯對苯二甲 酸酯(PET)、聚乙烯萘酸酯(PEN)、聚醯胺、聚 醯胺亞胺等之薄膜者。必要時亦可添加塡充物A 1、C a 、S i、T i、等之氧化物、碳酸鹽等之無機化合物,丙 烯樹脂系微粉末等之有機化合物等等。該薄膜中心P E T 、PEN、芳香族聚醯胺爲佳,更理想者以PET或PE N之2種或3種多層擠壓後複合化薄膜者佳。該彎曲性支 撑體可預先藉由電暈放電處理、等離子體放電及/或聚合 處理,易粘合劑塗佈處理.、除麈處理、熱及/或調濕後進 行緩和處理等亦可。一般彎曲性支撑體2之厚度爲5〜 1 0 0 # m 者。, 製造本發明硏磨層形成用塗料時,分散機以球磨機、 磨碎機、混砂機使用者爲宜。分散後之塗料中以設置過濾 工程者爲宜。硏磨層形成用塗料中若存在無機質粉體之未 分散物、凝聚物或樹脂不溶物等,則形成硏磨層塗膜時, 出現缺失、造成被硏磨物損傷之因。又,過濾工程係以去 ^ϋ n^i nn I ^ n^i ml .^n ml 、一OJ '- (諳先閱讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) A4規格(2丨0X297公釐) -13- A7 B7 五、發明説明(η ) 除硏磨層形成用塗料中之異物爲目的者。 製造硏磨帶時,由卷取滾壓連續成型薄膜狀之非磁性 支撑體上必要時混合硬化劑之同時(或混合)塗料藉由過 濾工程經一定過濾精度之過濾器過濾之後,可藉由 照相 凹版塗佈、逆輥塗佈,擠壓噴嘴塗佈等公知之各種塗佈方 法使塗佈硏磨層形成用塗料。 通常,塗料於塗佈前之彎曲挥支撑體2爲洗滌及表面 調整等目的,以水、溶劑等之濕式洗滌;不織布、極微細 纖維織物等做·爲兩刷使用之乾式洗滌;壓榨空氣、真空、 離子化空氣等非接觸式洗滌等公知之各種方法進行彎曲性 支撑體之前處理。爲提昇塗料與可撓性支撑體之密接性、 塗佈面爲目的下,亦可進行電暈放電、紫外線照射、電子 線照射等公知之各種非接觸表面處理。 ‘經濟部中央標準局員工消費合作社印製 (讀先閱讀背面之注意事項再填寫本頁) 於彎曲性支撑體2塗佈之硏磨層形成用塗料一般設置 於乾燥爐等之內部經熱風、遠紅外線、電熱器、真空裝置 等之公知之乾燥及蒸發方法而乾燥之。乾燥溫度爲4 0〜 200 °C、較隹60〜180 °C,更佳爲80〜150 °C 者依其彎曲性支撑體之耐熱性、溶劑種類、固形份濃度等 不同做適當選擇。當乾燥溫度小於4 0°C時,乾燥效率減 低,殘留溶劑量增,反之,超出2 0 0 °C則硏磨層塗膜中 之溶劑急劇蒸發,導致硏磨層表面粗細度劣化。又,亦可 配合乾燥爐內之溫.度,乾燥爐內之氣體通常利用空氣或不 活化氣體等即可。 將此硏磨層3乾燥後,爲促使硏磨層硬化,亦可進行 本紙張尺度適用中國國家標準(CNS > A4規格(210X297公釐) 14 - A7 B7 五、發明説明(12 ) 4 0 °C〜8 0 °C之熱硬化處理及/或霉子線照射處理。 再做所定形狀之切斷加工後,進行二次加工,而製成 本發明之硏磨帶。 以下代表本發明之具體實施例,更爲本發明做詳細說 明。惟,本發明並非僅限於此實施例中。 (實驗例1 ) 首先依以下重點製造聚酯聚胺酯樹脂。 (聚酯聚胺酯樹脂之製造) 於備有溫度計、攪拌器及部份環流式冷卻器之反應容 器中,加入二甲基對苯二甲酸酯、二甲基異苯二甲酸酯、 二醇,新戊二醇、醋酸鋅、醋酸鈉、於140 °C〜220 °C下進行3小時之酯交換反應。 再使反應系減壓至20分5mmHg,其間使昇溫至 250°C。更於0 . ImmHg,25〇°C下進行縮聚反 應60分鐘後,取得聚酯二醇(1) »其組成爲對苯二甲 經濟部中央標準局員工消費合作社印製 --------装! (讀先閱讀背面之注『意事項再磧寫本頁) 酸/異苯二甲酸/乙二醇/新戊二醇=5 0/ 5 0/5 0 /5 0 (莫耳比)者。 同法取得聚酯二醇(2)。其組成爲己二酸/1 ,4 一丁二醇/新戊二醇=1 0 0 / 7 5/2 5 (莫耳比)者 〇 於備有溫度計、攪拌器及環流式冷卻器之反應容器中 ,加入甲苯、甲基異丁酮,該聚酯二醇(1)、該聚酯二 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐〉-15- 經濟部中央標準局員工消費合作社印製 A 7 B7 五、發明説明Ο3 ) 醇(2)、4,4 > -二苯基甲烷二異氰酸酯、新戊二醇‘ 、二丁錫二月桂酸酯後,於7 0〜9 0°C下反應8小時後 分別製造出如表1所示之具數平均分子量(Μη )及玻璃 轉移溫度(T g )之各種聚酯聚胺酯樹脂。 再依下述要點製作硏磨層形成用塗料。 <硏磨層形成用塗料> (1 )粘合劑(結合劑)溶液之調整-· Polyurethane resin with S amount Mn of 200 0 OSMnSi 000 0 0 is contained as an essential component. The phenoxy resin used in the present invention is a nested molecular weight polyhydroxy polyether synthesized from bisphenol A and epichlorohydrin. The chemical structure is the same as that of epoxy resin, but it is compared with the epoxy resin generally used. Tree hire, its molecular weight is extremely large. . '一 I In —m —Mt n I4H nn · — nt ^^' Please read the two notes before you fill in this page). This paper size applies the Chinese National Standard (CNS) A4 specification (2) 〇x29Tifrt ), g_ A7 B7 V. Description of the invention f) And the number average molecular weight M η of the phenoxy resin used in the present invention is more than 10,000, especially those with 10,000 or more and 30,000 or less are ideally applicable. If a general epoxy resin is used, its number average molecular weight is 100 or less, and the strength of the coating film cannot be fully obtained, and problems such as peeling of the coating film of the honing layer are likely to occur. Among them, the average molecular weight is measured by a so-called standard polystyrene method. The phenoxy resin is a content of 5 to 70% by weight of the total amount of the binder, preferably 10 to 60% by weight, and more preferably 10 to 50% by weight. When the content is less than 5% by weight, the coating film strength of the honing layer will decrease, and problems such as peeling of the coating film of the honing layer will appear. On the other hand, if the content is more than 70% by weight, the coating film of the honing layer becomes hard and brittle and has no softness, causing the cause of damage to the honing material. Specific examples of the phenoxy group used in the present invention are, for example, Phenoxy 8 5500;-65 phenoxy resin company's "? Rule 11 (:", "PKHH", "PKHJ" and so on. These all meet The range of the above-mentioned ideal number average molecular weight. I Printed by the consumer cooperation of the Central Bureau of Standards of the Ministry of Economic Affairs (please read the precautions on the back before filling this page). ^ The amount Mη is 20000SMnl00000, preferably a polyester polyurethane resin of 2000 OSMnS 8 0 0 0 as an essential component. A polyester polyurethane resin having the number average molecular weight Mη is contained in the honing layer. It can improve the dispersibility of the coating for forming the honing layer, so that the honing layer formed by the coating has excellent honing characteristics. '(X, the number average molecular weight of the polyester polyurethane resin Mη is less than 2 0 0 0 0 Μ, the size makes 硏Reduced coating strength of abrasive layer, film fall of honing layer, etc. This paper size applies Chinese National Standard (CNS) A4 specification (210X297 mm) -7- Printed by A7 B7, Consumer Cooperative of Central Standards Bureau, Ministry of Economic Affairs , Invention description households). If the average molecular weight Mη is greater than 10,000, the dispersion of the coating for forming the honing layer will be reduced, resulting in deterioration of the surface of the honing layer and causing damage to the honing material during the honing operation. Content of the polyester polyurethane resin 30% to 95% by weight, preferably 40% to 90% by weight, and more preferably 50% to 90% by weight of the adhesive. The polyester polyurethane resin content exceeds 95% by weight and then honed The strength of the coating film decreases, and the coating film of the honing layer falls off. Conversely, if the content is less than 30% by weight, the coating film of the honing layer becomes hard and brittle and has no softness. It is easy to cause honing during honing In addition, the glass transition temperature T g of the polyester polyurethane resin is -50. (: STgS80 ° C, preferably -5p ° CSTgS + 4〇t :, more preferably -4 5 ° CSTgS +2 0t range. 1. When the glass transition temperature is too low, the strength of the honing layer coating film is reduced, and the honing capacity is reduced. On the other hand, if the glass transition temperature T g is too high, the honing layer coating film is hard and brittle, showing no The state of softness causes damage to the object to be honed during honing operation. In addition, the glass transfer of this resin is 1 degree T g based on値 measured by a dynamic viscoelasticity measuring device. The polyester polyurethane resin used in the present invention is a compound obtained by reacting a polyester diol with an isocyanate and a desired chain extender. The polyester used in the present invention Polyurethane resins are those that react organic diisocyanate (A), polyester diol (B) with a molecular weight of 500 to 50,000, and a chain extender ((:) with a molecular weight of 500 or less. Polyester polyurethane ^ Diisocyanate (»A) used in the resin manufacturing, for example: 2,4-toluene diisocyanate, 2,6-toluene This paper size is applicable to Chinese national standards (CNS > A4 specifications (210X 297 mm) _ ft-':-_____________ D *. T {Please read the note t on the back and fill in & this page) · Printed by the Shellfish Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs A7 B7 V. Description of the invention-) Brewing monoisocyanate, p-phenylene diisocyanate, diphenylmethyl diisocyanate, m-phenylene diisocyanate, hexamethylene diisocyanate, tetramethylene monoisocyanate, 3 '3 —dimethoxy-4,4-—bisfluorene diisocyanate, 2,4- Diisocyanate, 3,3-Dimethyl-1 4 '4 / monobisene diisocyanate, -4,4 < monodiene diisocyanate, 4,4 / --diisocyanate diphenyl ether, 1,5 —Naphthalene diisocyanate, p-xylene diisocyanate, m-xylene diisocyanate '1' 3-diisocyanate methylcyclohexane, 1,4-diisocyanate methylcyclohexane, 4, 4 / Examples of diisocyanate cyclohexane, 4,4-- diisocyanate cyclohexanemethane, isoflurone diisocyanate, and the like. Examples of the polyester diol (B) used in the production of the polyester polyurethane resin are those having a molecular weight in the range of 500 to 50,000. Examples of the carboxylic acid components of polyester diols are: aromatic dicarboxylic acids such as terephthalic acid, isophthalic acid, phthalic acid '1' 5-naphthalenedicarboxylic acid, p-oxybenzoic acid, p-- Examples of aromatic oxycarboxylic acids such as (hydroxyethoxy) benzoic acid; aliphatic dicarboxylic acids such as succinic acid, adipic acid, azelaic acid, sebacic acid, and lauric acid. Among them, terephthalic acid, isophthalic acid, phthalic acid, 'adipic acid, and sebacic acid are particularly preferable. In addition, the glycol component of polyester diol is, for example, ethylene glycol, propylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, neopentyl Diethylene glycol, diethylene glycol, dipropylene glycol, 2,2,4-trimethyl-1, .. 3-pentanediol, cyclohexanedimethanol, bisphenol A ethylene oxide additives and propylene oxide Additives, hydrogenated bisphenol A ethylene oxide additives and propylene oxide additives, etc. This paper size applies Chinese National Standard (CNS) A4 specification (210X 297 mm) -9-(谙 Read the precautions on the back before filling in this page) Binding · Ordering A7 B7 Printed by the Staff Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs 、 Instructions of the invention P.) 1 1 Other examples of this polyester diol: δ — Caprolactones such as caprolactone after opening TSt bad 1 1 | Examples of lactone polyester diols obtained after polymerization 〇1 1 The long-chain diol (B), as described above, is used to improve the mechanical properties of the polyester polyurethane resin. It is a polyester diol with a molecular weight of 5.0 0 5 5 0 0. It is recommended to use 1 1 if the molecular weight is less than 5 0 0 The concentration of the amine ester group is too high. The resin is soft in the back 6 1 I Properties > Solvent solubility is reduced to produce a bad situation. 0 Conversely, the molecular weight is too large to pay attention. Too low low-polyester polyurethane resin special feature 1 has strong toughness and wear resistance Unsatisfactory 0 Filling; the chain extender (C) with a molecular weight less than page 1 1 5 0 0 used in the manufacture of polyester polyurethane resin contains more than 2 active hydrogens in 1 molecule 1 1, S field m After the concentration of urethane group or urethane group in the polyester polyurethane resin is adjusted, a unique strong toughness effect is attached to the polyester 1 polyurethane. The specific compound of the chain extender (C) such as ethylene glycol, 1 3 1 1 I — propylene glycol, 1 4 — butanediol 1 6 — hexanediol> cyclohexanedimethyl 1 1 alcohol xylene glycol, diethylene glycol triethylene glycol, bisphenol A ethylene oxide 1 alkane addition Straight-chain diols such as propylene glycol & neopentyl glycol > 1 2 monobutyl- * | — alcohol 1 3 — butanediol% 2 2 4 — trimethyl-1 3 _ 1 I pentanediol, bis Branched diol monoethanol of phenol A propylene oxide addition 1 1 I Amine \ Amine alcohol such as n-methylethanolamine, ethyl Diamine% Hexamethylenediamine 1 > Diamines such as isoflurone diamine or hydrogen, etc. 0 1 1 Ideal for the polyester polyurethane resin of the present invention, such as polyester di 1 | alcohol (1 ) / Polyesterdiol (2) / neopentyl glycol / 4 4 diphenylbenzene 1 I The reaction product of the methyl isocyanate diisocyanate, the example of polyesterdiol (1) 1 1 I such as: terephthalene Formic acid / isophthalic acid / ethylene glycol / neopentyl glycol 1 1 This paper size applies to the Chinese National Standard (CNS) A4 format (210X297 mm) -10- Du Yinju A 7 B7 V. Explanation of the invention) 50/50/50/50 Morse ratio, for example, polyester diester (2): adipic acid / 1,4-butanediol / neopentylene glycol = 10.00 / 7 5/2 5 Morse. In addition, by controlling the blending ratio of the polyester diol (1) / polyester diol (2) and the concentration of the amine ester group, the glass transition temperature Tg of the polyester polyurethane resin can be arbitrarily controlled. The amount of the binder contained in the honing layer (coating material for forming a honing layer) is 5 to 50 parts by weight of 100 parts by weight of the inorganic powder contained in the honing layer, and particularly 10 to 40 weight. Sharers are good. When the content of the binder is less than 5 parts by weight, the strength of the coating film of the honing layer will be reduced, and the coating film of the honing layer will fall off. Conversely, if the content of the binder is more than 50 parts by weight, the content of the inorganic powder will be reduced, resulting in poor honing characteristics. As examples of the cross-linking agent for hardening the binder, various polyisocyanates, particularly diisocyanates, are preferably used with more than one tolyl diisocyanate, hexamethylene diisocyanate, and methylene diisocyanate. . This cross-linking agent is preferably a cross-linking agent denatured with a plurality of hydroxyl groups such as trimethylolpropane or a triisocyanate-type cross-linking agent in which three molecules of a diisocyanate compound are combined. The cross-linking agent is a resin cross-linked with a functional group or the like contained in the adhesive. The content of the crosslinking agent is preferably 10 to 30 parts by weight based on 100 parts by weight of the binding agent. Hardening heat The hardening resin is usually heated in a heating oven at 40 to 80 ° C for 1 to 4 to 8 hours. As an inorganic powder contained as a necessary component in the coating for forming the honing layer (honing layer), users with a Mohs hardness of 5 or higher are advised to use it. 'For example: carbonized paper standards are applicable to China National Standard (CNS) A4 specifications ( 210X297mm) -11-~ ", two Γ m ml 1V1 I tm · —1 ^ —fv I t , T-(Please read the precautions on the back before filling the 1ΪΤ page) A7 ______ B7 V. Description of the invention $ ) Fine powders of silicon, aluminum oxide, silicon nitride, chromium oxide, chromium oxide, diamond, emery, etc. are used alone or in combination of two or more types. Among them, silicon carbide or alumina users are more ideal. The particle size of the inorganic powder is preferably 0.1 ~ 2 0 Am, and the specific particle size that is practically supplied can be selected to be included in the actual rough scraping or processing honing purpose. If the particle size is less than 0.1 Am, the honing function will be insufficient for processing honing. Conversely, if it is larger than 20 / zm, the problem of damage to the honing object during rough scraping will occur. Also, in the honing layer of the present invention, as an additive, if necessary, the user has a lubricating effect, an antistatic effect, a dispersing effect, and a plasticizing effect. Specific examples include fatty acids, fatty acid esters, and silicone oils. , Fluorine oil, various surfactants, carbon black, etc. can be added. Printed by the Consumers 'Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs --- ^ ------'. One Pack ---'- (锖 Read the precautions on the back before filling this page) as a honing layer For organic solvents used in coatings, such as: ketones such as methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, aromatic hydrocarbon groups such as toluene and xylene, and esters such as ethyl acetate and butyl acetate Or use these mixed solvents at any ratio. Among them, those having a high boiling point solvent containing cyclohexanone are preferred because they can form a good honing layer. Cyclohexanone is contained in an amount of 20 to 60% by weight in the total organic solvent, more preferably 25 to 50% by weight. Within this range, good surface quality of the honing layer can be obtained, the honing function can be improved, and the occurrence of scratches on the honing layer can be prevented. The solid content concentration of the coating for forming the honing layer is preferably from 30 to 70% by weight, and more preferably from 40 to 60% by weight. If the ratio is less than 30% by weight, the honing layer is formed. The amount of residual solvent will increase, making it impossible to obtain a uniform coating film and other undesirable conditions. Conversely, if it is greater than 70% by weight, the size of the coated paper applies the Chinese National Standard (CNS) A4 specification (210X297 mm) -12 · Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs A7 B7 V. Invention Description 彡 〇) The viscosity of the material increases, and the coating film of the honing layer dries too fast to obtain uniform sentences. The coating film is not ideal. The film thickness of the honing layer 3 is selected according to the shape and material of the object to be honed. Generally, it is 3 ~ 25 / zm, and more preferably 5 ~ 20em. If the film thickness is less than 3, the elasticity of the coating film will disappear because the film thickness is too thin. Honing operation is easy to damage and to be honed. Conversely, if it is too large beyond 2 5 # m, honing-scratches are likely to occur during honing operations. Honing layer 3-Generally, it can be formed by coating alone, or two or more layers. As the flexible support 2 used in the present invention, a film such as polyethylene terephthalate (PET), polyvinyl naphthalate (PEN), polyamide, polyimide, or the like can be used. If necessary, inorganic compounds such as oxides, carbonates, etc. of the fillers A1, Ca, Si, Ti, etc., organic compounds such as acrylic resin fine powder, and the like may be added. The film center is preferably P E T, PEN, or aromatic polyamidamine. More preferably, two or three layers of PET or PE N are laminated to form a composite film. The flexible support may be subjected to a corona discharge treatment, a plasma discharge and / or a polymerization treatment in advance, an easy adhesive coating treatment, a descaling treatment, a heat treatment and / or a damping treatment, and then a relaxation treatment. Generally, the thickness of the flexible support 2 is 5 to 100 mm. When manufacturing the coating for forming the honing layer of the present invention, the user of the dispersing machine is preferably a ball mill, a grinder, or a sand mixer. It is advisable to install a filtering process in the dispersed paint. If there are undispersed inorganic powders, aggregates, or resin-insoluble matter in the coating for forming the honing layer, the formation of the honing layer coating film may cause a loss and damage to the honing material. In addition, the filtration engineering is to remove ^ ϋ n ^ i nn I ^ n ^ i ml. ^ N ml, one OJ '-(谙 Please read the precautions on the back before filling this page) This paper size applies Chinese national standards (CNS ) A4 specification (2 丨 0X297 mm) -13- A7 B7 V. Description of the invention (η) The purpose is to remove the foreign matter in the coating for honing layer formation. When manufacturing honing belts, the non-magnetic support is continuously formed by rolling and rolling. When necessary, the hardener is mixed at the same time (or mixed). The coating is filtered by a filter with a certain filtration accuracy. Various coating methods such as gravure coating, reverse roll coating, and extrusion nozzle coating are used to coat the coating for forming a honing layer. Generally, the curved support 2 of the coating before coating is used for washing and surface adjustment purposes, wet washing with water, solvent, etc .; non-woven fabrics, ultra-fine fiber fabrics, etc. · dry washing for two brushes; squeezing air Various methods known in the art, such as non-contact washing such as vacuum, ionized air, etc., are used to perform the pretreatment of the flexible support. For the purpose of improving the adhesion between the paint and the flexible support, and the coating surface, various known non-contact surface treatments such as corona discharge, ultraviolet irradiation, and electron irradiation can be performed. 'Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs (read the precautions on the back and then fill out this page) The coating for forming the honing layer applied to the flexible support 2 is generally installed inside a drying furnace, etc. Far-infrared rays, electric heaters, vacuum devices, and other known drying and evaporation methods. The drying temperature is 40 ~ 200 ° C, more than 隹 60 ~ 180 ° C, more preferably 80 ~ 150 ° C. Depending on the heat resistance of the flexible support, the type of solvent, and the concentration of solid content, etc., it should be appropriately selected. When the drying temperature is less than 40 ° C, the drying efficiency decreases and the amount of residual solvent increases. On the other hand, when it exceeds 200 ° C, the solvent in the honing layer coating film evaporates rapidly, resulting in deterioration of the surface roughness of the honing layer. In addition, the temperature in the drying furnace can also be matched. Generally, the gas in the drying furnace can be air or inactivated gas. After drying the honing layer 3, in order to promote the hardening of the honing layer, the Chinese paper standard (CNS > A4 (210X297 mm)) can be applied to this paper size. 14-A7 B7 V. Description of the invention (12) 4 0 ° C ~ 80 ° C heat curing treatment and / or mold line irradiation treatment. After the cutting process of the predetermined shape is performed, the secondary processing is performed to make the honing belt of the present invention. The following represents the specifics of the present invention Examples, the present invention will be described in more detail. However, the present invention is not limited to this example. (Experimental Example 1) First, a polyester polyurethane resin is manufactured according to the following points. (Production of polyester polyurethane resin) A thermometer is provided. In the reaction vessel of the stirrer and part of the circulating cooler, add dimethyl terephthalate, dimethyl isophthalate, glycol, neopentyl glycol, zinc acetate, sodium acetate, The transesterification reaction was performed at 140 ° C ~ 220 ° C for 3 hours. The reaction system was decompressed to 20 minutes and 5 mmHg, and the temperature was increased to 250 ° C. The polycondensation reaction was performed at 0.1 mmHg and 25 ° C. After 60 minutes, polyesterdiol (1) was obtained Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs -------- installed! (Read the note on the back of the "Issue and then write this page") Alcohol = 5 0/5 0/5 0/5 0 (Mole ratio). Polyester diol (2) was obtained in the same way. Its composition is adipic acid / 1,4 butanediol / neopentyl glycol. = 1 0 0/7 5/2 5 (mole ratio) 〇 To a reaction vessel equipped with a thermometer, a stirrer and a circulation cooler, add toluene and methyl isobutyl ketone. The polyester diol (1 ), The second polyester paper size is applicable to Chinese National Standard (CNS) A4 specifications (210X297 mm> -15- printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs A 7 B7 V. Description of the invention 〇3) Alcohol (2) 4,4 > -Diphenylmethane diisocyanate, neopentyl glycol ', dibutyltin dilaurate, reacted at 70 ~ 90 ° C for 8 hours, and produced as shown in Table 1 Various polyester polyurethane resins having a number average molecular weight (Μη) and glass transition temperature (Tg). Then, a coating for forming a honing layer is prepared according to the following points. ≪ Coating for forming a honing layer > (1) Adhesion Agent Mixture) of the solution was adjusted

•苯氧基樹脂+ (Phenoxy Associates社製 PKHH 數平均分子量=1 5 0 0 0 ) ......... 2 0重量份 •聚酯聚胺酯樹脂(具備表1所示之數平均分子量Μη及 玻璃轉移溫度T g之物性)…···…8 0重量份 • Μ E K (丁酮)………1 3 0重量份 ·.甲苯.........1 3 0重量份 •環己酮.........1 4 0重量份 將該組成物投入超高混合.器中,進行6小時混合攪拌 後做成粘合溶液。該粘合溶液以9 5 %剪切過濾精度= 1 5 . 0 //m之深度濾器使用後,進行8小時之循環過濾 〇 · (2 )分散處理 •無機質粉體(氧化銘,Fujuincopoleted社製 WA#4 0 0 0 ) ......... 5 0 0 重量份 •粘合溶液(上記所述者).........5 0 0重量份 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)-16· (請先閱讀背面之注意事項再填本頁)• Phenoxy resin + (PKHH number average molecular weight manufactured by Phenoxy Associates = 15 0 0 0) ......... 20 parts by weight • Polyester polyurethane resin (with the number average molecular weight shown in Table 1) Physical properties of Μη and glass transition temperature T g) ..... 8 0 parts by weight. Μ EK (butanone) ... 1 3 0 parts by weight ... toluene ... 1 3 0 parts by weight Parts • Cyclohexanone ... 140 parts by weight of this composition is put into an ultra-high mixing device, mixed and stirred for 6 hours to prepare an adhesive solution. This binding solution was cut with 95% shearing filtration accuracy = 15.0. After using the depth filter, it was subjected to 8-hour cycle filtration. (2) Dispersion treatment • Inorganic powder (Oxide Ming, manufactured by Fujuincopoleted) WA # 4 0 0 0) ......... 5 0 0 parts by weight • Adhesive solution (described above) ......... 5 0 0 parts by weight This paper is applicable to China National Standard (CNS) A4 Specification (210X297mm) -16 · (Please read the precautions on the back before filling this page)

*1T 經濟部中央標準局員工消費合作社印製 A 7 __B7_ 五、發明説明(14 ) 將該組合投入磨碎機後,進行3小時分散。 (3 )粘度調整 完成該分散處理後,更投入下記之溶劑後,再進行1 小時分散之。 .Μ E K (丁酮.........7 0重量份 •甲苯.........70重量份 •環己酮.........8. 0重量份 將該粘度調整後之硏磨層形成用塗料利用9 5 %剪切 過濾精度=2 5 · 0/zm之深度濾器後進行8小時之循環 過濾。 (4 )最終塗料 於過濾後之塗料12 2 0重量份中加入異氰酸酯化合 物(日本聚胺酯工業社製、ColonateL ) 2 0重量份後,攪 拌混合後,做成硏磨層形成用塗料。 (硏磨帶之製怍·) 於7 5; m厚之聚乙烯對苯二甲酸酯薄膜組成之彎曲 性支撑體之單側表面上塗佈該硏磨層形成用塗料後乾燥之 。乾燥後之硏磨層膜厚度爲1 5 。完成塗佈乾燥之滾 壓於6 0 °C之加熱.烤箱使硬化2 4小時後,切成3 / 4 i n c h寬後,製成硏磨帶試驗品。 製成下表1所示之各種硏磨帶試驗品後,各硏磨帶樣 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)-17 - (討先閱讀背面之注^-事碩再填艿本頁)* 1T Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs A 7 __B7_ V. Description of the invention (14) After putting the combination into the grinder, it was dispersed for 3 hours. (3) Viscosity adjustment After the dispersing treatment is completed, the following solvent is added, and dispersing is performed for 1 hour. .Μ EK (Butanone ......... 7 0 parts by weight • Toluene ......... 70 parts by weight • Cyclohexanone ......... 8 weight The coating for forming the honing layer after adjusting the viscosity was subjected to 8-hour cycle filtration using a depth filter with a 95% shear filtration accuracy = 2 5 · 0 / zm. (4) The final coating was filtered after the coating 12 20 parts by weight was added an isocyanate compound (ColonateL, manufactured by Japan Polyurethane Industry Co., Ltd.). After 20 parts by weight, the mixture was stirred and mixed to form a coating for forming a honing layer. (Made by honing belt ·) at 7 5; m The honing layer-forming coating is coated on one side of a flexible support composed of a thick polyethylene terephthalate film and then dried. The dried honing layer has a film thickness of 15 and the coating is completed. The dried rolls were heated at 60 ° C. The ovens were hardened for 24 hours, and then cut into 3/4 inch widths to make honing belt test pieces. Various honing belt tests were made as shown in Table 1 below. After the product is finished, the paper size of each honing belt sample applies to the Chinese National Standard (CNS) A4 specification (210X297 mm) -17-(Please read the note on the back ^-matter master before filling this page)

A7 A7 ........ •完好無缺 0 ··· _· •具有1〜 2條傷痕 ,尙可達製品之水準者。 Δ........ •具有3〜 5條傷痕 ,做爲製品之水準尙可。 X ........ •具6條以上傷痕, 做爲製品爲次級水準者。 經濟部中央標準局員工消費合作社印製 —______B7__ 五、發明説明(|5 ) &依下述重點分別評定其相對硏磨能,磁頭硏磨損傷,以 及硏磨帶刮傷等特性之測定。 相對硏磨能 將純粒鐵磁頭利用硏磨帶樣品硏磨後,求取硏磨純粒 鐵磁頭1 // m所須時間。此硏磨時間針對N 0 .樣品1之 硏磨時間之相對値示之。亦即.,基準樣品N 0 . 1之硏磨 能爲1 0 0時所做成之相對値。小於1 〇 〇之値者其硏磨 能愈優異,。 to頭硏磨傷 將純粒鐵以硏磨帶樣品硏磨後,以光學顯微鏡觀察形 成於磁頭表面之損傷狀態,以下述做爲判定基準。 硏磨帶刮傷 將純粒鐵利用硏磨帶樣品硏磨時,以光學顯微鏡觀察 其硏磨帶之硏磨層是否出現刮傷,以下述做爲判定基準評 定之。 〇.........未有刮痕出現。 △.........具輕度刮傷,尙達製品水準者。 本紙張尺度適用中國國家標準(CNS > A4規格(2丨0X297公釐)—~- 1R - {請先閲請背面之注意事項再填寫本頁}A7 A7 ........ • Intact 0 ··· _ · • Have 1 ~ 2 scars, which can reach the level of the product. Δ ........ • It has 3 ~ 5 scars, which is a good standard for products. X ........ • With 6 or more scars, as a product with a secondary level. Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs —______ B7__ V. Description of the Invention (| 5) & The characteristics of relative honing energy, magnetic head honing damage, and honing belt scratching were measured according to the following points. Relative Honing Energy After honing a pure-grain ferromagnetic head using a honing belt sample, find the time required to honing the pure-grain ferromagnetic head 1 // m. This honing time is shown relative to the honing time of N 0. Sample 1. That is, the relative honing made when the honing energy of the reference sample N 0.1 is 100. Those who are less than 1,000 have better honing ability. To head honing abrasion After grinding pure grain iron with a honing belt sample, observe the damage state formed on the surface of the magnetic head with an optical microscope, and use the following as a criterion for judgment. Honing belt scratches When honing the pure grain iron with a honing belt sample, observe whether the honing layer of the honing belt is scratched with an optical microscope, and evaluate it with the following criteria. 〇 ......... No scratches appear. △ ......... has a slight scratch and reaches the product level. This paper size applies to Chinese national standards (CNS > A4 size (2 丨 0X297mm) — ~-1R-{Please read the notes on the back before filling this page}

A7 B7五、發明説明(16 )X .........具明顯刮傷,爲次級製品。以上測定結果示於下表1。 (請先閲請背面之注意事項再填巧本頁) 訂 經濟部中央標率局員Η消費合作社印製 本紙張尺度適用中國國家標準(CNS ) Α4規格(210X297公釐)-19 - 經濟部中央標準局員工消費合作社印製 396087 A7 B7 五、發明説明(/;?) 表1A7 B7 V. Description of the invention (16) X ......... has obvious scratches and is a secondary product. The above measurement results are shown in Table 1 below. (Please read the notes on the back before filling in this page.) Ordered by the Central Standards Bureau of the Ministry of Economic Affairs and printed by the Consumer Cooperatives. This paper applies the Chinese National Standard (CNS) Α4 specification (210X297 mm) -19-Central Ministry of Economic Affairs Printed by Standards Bureau Consumer Cooperatives 396087 A7 B7 V. Description of Invention (/ ;?) Table 1

樣品No. 聚酯聚胺酯 苯氧基/聚酯 相對. 磁頭 硏磨帶 Μη Tg(°C) 聚胺酯 硏磨能 硏磨傷 刮痕 (重量比) 1 49000 -30 20/80 100 ◎ 〇 2 25000 -30 20/80 99 ◎ 〇 3 70000 -30 20/80 , 101 ◎ 〇 4 90000 -30 20/80 105 〇 〇 5(比較) 10000 ' -30 20/80 140 ◎ X 6(比較) 150000 -30 20/80 120 X 〇 7 49000 -45 20/80 110 ◎ 〇 8 49000 20 20/80 98 ◎ 〇 9 49000 40 20/80 95 〇 〇 10 49000 70 20/80 88 Δ 〇 11 49000 -30 5/95 110 ◎ △ 12 49000 -30 10/90 106 ◎ 〇 13 49000 -30 40/60 97 ◎ 〇 14 49000 -30 50/50 90 ◎ 〇 15 49000 -30 60/40 88 〇 〇 16 49000 -30 70/30 80 △ 〇 17(比較) 49000 -30 20/80 120 ◎ X 樣品No.l7:樣品No」之苯氧基樹脂以環氧樹脂(Μ η = 6000)取代使用之 I--------ί 裝-- U · (讀先閱請背面之注意事項再填寫本頁) 本纸張尺度適用中國國家標準(CNS ) Α4規格(210X297公釐) 396087 A7 B7 經濟部中央標準局員工消費合作社印製 五、發明説明(18 ) (實驗例2 ) / 上述實驗例中使用硏磨帶精品1、 5及6,備用後, 硏磨易彎性磁碟片後’評定磁碟片表面之損傷及硏磨帶刮 痕之特性後,其結果示於下表2。 磁碟片硏磨傷 ' 將易彎性磁碟片以硏磨帶樣昂硏磨後,經光學顯微鏡 觀察形成於磁片表面之損傷狀況,以下述做爲判定基準評 定之。' 〇.........定好無缺 X .........傷痕產生、爲次級製品 硏磨帶刮痕 將易彎性磁碟片利用硏磨帶Sample硏磨後,以光學顯 微鏡觀察於硏磨帶之硏磨層是否有刮痕出現。下述爲判定 基準評定之。 〇.........未出現刮痕 X .........出現刮痕,爲次級製品 測定結果示於下表2。 (請先閲讀背面之注意事項再填#?本頁) *-° 本紙張尺度適用中國&家標準(CNS ) A4規格(210X297公釐) 21 _ A7 B7 396087 五、發明説明(>9 ) 表2Sample No. Polyester polyurethane phenoxy / polyester relative. Magnetic head honing belt Μη Tg (° C) Polyurethane honing can abrasion scratches (weight ratio) 1 49000 -30 20/80 100 ◎ 〇2 25000- 30 20/80 99 ◎ 〇3 70000 -30 20/80, 101 ◎ 〇4 90000 -30 20/80 105 〇5 (comparative) 10000 '-30 20/80 140 ◎ X 6 (comparative) 150000 -30 20 / 80 120 X 〇7 49000 -45 20/80 110 ◎ 〇8 49000 20 20/80 98 ◎ 〇9 49000 40 20/80 95 〇〇10 49000 70 20/80 88 Δ 〇11 49000 -30 5/95 110 ◎ △ 12 49000 -30 10/90 106 ◎ 〇13 49000 -30 40/60 97 ◎ 〇14 49000 -30 50/50 90 ◎ 〇15 49000 -30 60/40 88 〇〇16 49000 -30 70/30 80 △ 〇17 (comparative) 49000 -30 20/80 120 ◎ X Sample No. 17: Sample No. The phenoxy resin is replaced by epoxy resin (M η = 6000) I -------- ί Installation-U · (Read the first read, please read the notes on the back, then fill out this page) This paper size applies to China National Standard (CNS) Α4 size (210X297 mm) 396087 A7 B7 Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economy Five 2. Description of the invention (18) (Experimental Example 2) / The honing belts 1, 5, and 6 were used in the above experimental examples. After the spare time, after honing the flexible disc, the damage and honing of the surface of the disc were evaluated. The results after scratching are shown in Table 2 below. Magnetic disk honing damage 硏 After bending a flexible magnetic disk with a honing belt, observe the damage formed on the surface of the magnetic disk with an optical microscope, and evaluate it with the following criteria. '〇 ...... determined without defect X ......... wounds generated, honing belt scratches for secondary products, after using the honing belt Sample for honing the flexible magnetic disc With an optical microscope, observe whether the honing layer on the honing belt has scratches. The following are the evaluation criteria. ○ ... No scratches occurred X ......... Scratches appeared, which is a secondary product. The measurement results are shown in Table 2 below. (Please read the notes on the back before filling #? This page) *-° This paper size applies to China & House Standard (CNS) A4 specification (210X297 mm) 21 _ A7 B7 396087 V. Description of the invention (> 9 ) Table 2

Sample 磁片表面 硏磨傷 研磨帶 刮傷 1 〇 〇 5 (比較) 〇 X 6 (比較) X 〇 由以上結果可淸楚証明本發明之效果。亦即,本發明 硏磨帶於彎曲性支撑體上以含無機質粉體及結合劑做爲主 成份之硏磨層之硏磨帶者,含於該硏磨層之結合劑係由 1) 苯氧基樹脂與Sample Surface of magnetic discs Abrasion Abrasive tape Scratch 1 〇 〇 5 (comparative) 〇 X 6 (comparative) X 〇 The above results can clearly prove the effect of the present invention. That is, if the honing belt of the present invention is a honing belt with a honing layer containing inorganic powder and a binder as main components on a flexible support, the binding agent contained in the honing layer is composed of 1) benzene Oxy resin with

2) 數平均分子量Μη爲2 OOOOSMnS 1 0 0 0 0 0之聚酯聚胺酯樹脂所組成者,因此可有效防 止被硏磨物(硏磨對象)表面產生硏磨損傷,減少硏磨帶 之硏磨層刮痕,同時,具有極佳之硏磨能力等效果均被發 現。2) A polyester polyurethane resin with a number average molecular weight Mη of 2 OOOOSMnS 1 0 0 0 0 0, so it can effectively prevent honing damage on the surface of the object to be honed (honed object) and reduce the honing of the honing belt Layer scratches, and at the same time, have excellent honing ability and other effects were found.

In I In —.K n In HI ^H - - n HI n) 1^11 一OJ J' (請先閱請背面之注意事項再填艿本頁) 經濟部中央標準局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐).22In I In —.K n In HI ^ H--n HI n) 1 ^ 11 One OJ J '(Please read the notes on the back before filling out this page) Printed by the Staff Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs Paper size applies to China National Standard (CNS) A4 (210X297 mm) .22

Claims (1)

396087 A8 B8 C8 D8 六、申請專利範圍 1 種硏磨帶,其特徵係於可撓性支撑體上具有以 含無機質粉體及結合劑做爲主成份之硏磨層之硏磨帶中, 於該硏磨層中所含之結合劑係由 1 )苯氧基樹脂與' 2 )數平均分子量Μη爲2 0 0 0 OSMn S 1 0 0 0 0 0之聚酯聚胺酯樹脂所組成者。 2 .如申請專利範圍第1項.之硏磨帶,其中該苯氧基 樹脂之數平均分子量爲大於1 0 〇 〇 〇之組成者。 3 .如申請專利範圍第1項之硏磨帶,其中該苯氧基 樹脂之數平均分子量爲1 0 0 00以上〜30000以下 者。 4 .如申請專利範圍第1項之硏磨帶’其中該苯氧基 樹脂與聚酯聚胺酯樹脂之重量配合比例爲5: 9 5〜70 : 3 0者。 5 .如申請專利範圍第1項之硏磨帶’其中該聚醋聚 胺酯樹脂之玻璃轉移溫度T g爲一 5 0°C〜8 〇°C者》 6 .如申請專利範圍第1項之硏磨帶’其中該無機質 粉體爲莫氏硬度5以上,粒徑0 . 1〜20/zm者。 (請先閲讀背面之注意事項再填寫未瓦) 裝· 訂 經濟部中央標準局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS > A4規格(210X297公釐) -23-396087 A8 B8 C8 D8 VI. Patent application scope 1 type of honing belt, which is characterized in that the flexible support has a honing layer containing inorganic powder and a binder as the main component of the honing belt. The binder contained in the honing layer is composed of 1) a phenoxy resin and a polyester polyurethane resin having a number average molecular weight Mn of 2 0 OSMn S 1 0 0 0 0 0. 2. The honing belt according to item 1 of the scope of the patent application, wherein the number average molecular weight of the phenoxy resin is a composition having a number greater than 100%. 3. The honing belt according to item 1 of the scope of patent application, wherein the number average molecular weight of the phenoxy resin is more than 10,000 to less than 30,000. 4. The honing belt according to item 1 of the patent application range, wherein the weight ratio of the phenoxy resin to the polyester polyurethane resin is 5: 9 5 to 70: 30. 5. As for the honing belt of item 1 in the scope of patent application, in which the glass transition temperature T g of the polyurethane resin is -50 ° C ~ 80 ° C. Abrasive belt 'wherein the inorganic powder has a Mohs hardness of 5 or more and a particle size of 0.1 to 20 / zm. (Please read the precautions on the back before filling in the tiles.) Binding and printing. Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs. This paper size applies to Chinese national standards (CNS > A4 size (210X297 mm) -23-
TW087104476A 1997-04-25 1998-03-25 Laping tape TW396087B (en)

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JP5831974B2 (en) * 2011-11-08 2015-12-16 Mipox株式会社 Sheet glass having edge polished by polishing tape, and method and apparatus for polishing sheet glass edge
MX340903B (en) * 2011-12-20 2016-07-29 Cytec Ind Inc Dry fibrous material for subsequent resin infusion.
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